Results 191 to 200 of about 6,468 (222)

Chromosomal Instability in Hereditary Tyrosinemia Type I

Pediatric Pathology, 1990
Enid Gilbert-Barness, Lorraine F Meißner   +1 more
exaly  

Increased nitric oxide release by neutrophils of a patient with tyrosinemia type III

Biomedicine and Pharmacotherapy, 2009
Patrizia D'Eufemia, R Finocchiaro, Mauro Celli   +2 more
exaly  

Tyrosinemia (TYRSN)

2023
Alireza Barzegary, Alireza Noroozi, Amirali Karimi, Nima Rezaei   +3 more
openaire   +1 more source

Prenatal Diagnosis of Tyrosinemia Type 1 Using Next Generation Sequencing

Fetal and Pediatric Pathology, 2016
Maryam Rafati, Saeed Reza Ghaffari
exaly  

Tyrosinemia type I treated by NTBC: How does AFP predict liver cancer?

Molecular Genetics and Metabolism, 2006
A van der Ploeg, M M van den Heuvel-Eibrink, F A Wijburg   +2 more
exaly  

Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin

Molecular Genetics and Metabolism, 2011
Faiqa Imtiaz, Mohamed S Rashed, Bashayer Al-Mubarak   +2 more
exaly  

Tyrosinemia

2008
openaire   +1 more source

Spectrum of mutations in the fumarylacetoacetate hydrolase gene of tyrosinemia type 1 patients in northwestern Europe and Mediterranean countries

Human Mutation, 1998
R Berger
exaly  

HEREDITARY TYROSINEMIA

Acta Paediatrica, International Journal of Paediatrics, 1969
G Bodegard, Bengt Lindblad, Sven Lindstedt   +2 more
exaly  

Tissue-specific FAH deficiency alters sleep–wake patterns and results in chronic tyrosinemia in mice

Proceedings of the National Academy of Sciences of the United States of America, 2019
Sandra M Siepka, Kimberly H Cox, Vivek Kumar   +2 more
exaly